Evidence map›Paper›PMID 30387018›Full record

ArticleChemistry Central journal2018

Design, synthesis, ADME prediction and pharmacological evaluation of novel benzimidazole-1,2,3-triazole-sulfonamide hybrids as antimicrobial and antiproliferative agents.

Fawzia Faleh Al-Blewi, Meshal A Almehmadi, Mohamed Reda Aouad, Sanaa K Bardaweel, Pramod K Sahu, Mouslim Messali, Nadjet Rezki, El Sayed H El Ashry

Abstract read
In one paragraph

Article in Chemistry Central journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Article
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  12. Nanoformulation-Based 1,2,3-Triazole Sulfonamides for Anti-Tropical medicine and infectious disease · 2023
    Article
  13. Review
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  20. Anti-COVID-19 activity of some benzofused 1,2,3-triazolesulfonamide hybrids usingChemometrics and intelligent laboratory systems : an international journal sponsored by the Chemometrics Society · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Fawzia Faleh Al-BlewiDepartment of Chemistry, Faculty of Science, Taibah University, Medina, 30002, Saudi Arabia.
Meshal A AlmehmadiDepartment of Chemistry, Faculty of Science, Taibah University, Medina, 30002, Saudi Arabia.
Mohamed Reda AouadDepartment of Chemistry, Faculty of Science, Taibah University, Medina, 30002, Saudi Arabia. aouadmohamedreda@yahoo.fr.
Sanaa K BardaweelDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, University of Jordan, Amman, 11942, Jordan.
Pramod K SahuSchool of Study in Chemistry, Jiwaji University, Gwalior, Madhya Pradesh, 474011, India.
Mouslim MessaliDepartment of Chemistry, Faculty of Science, Taibah University, Medina, 30002, Saudi Arabia.
Nadjet RezkiDepartment of Chemistry, Faculty of Science, Taibah University, Medina, 30002, Saudi Arabia.
El Sayed H El AshryDepartment of Chemistry, Faculty of Science, Alexandria University, Alexandria, 21500, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNitrogen heterocyclic rings and sulfonamides have attracted attention of several researchers.

resultsA series of regioselective imidazole-based mono- and bis-1,4-disubstituted-1,2,3-triazole-sulfonamide conjugates 4a-f and 6a-f were designed and synthesized. The first step in the synthesis was a regioselective propargylation in the presence of the appropriate basic catalyst (Et

conclusionIn summary, we have successfully synthesized novel targeted benzimidazole-1,2,3-triazole-sulfonamide hybrids through 1,3-dipolar cycloaddition reactions between the mono- or bis-alkynes based on imidazole and the appropriate sulfonamide azide under the optimized Cu(I) click conditions. The structures of newly synthesized sulfonamide hybrids were confirmed by means of spectroscopic analysis. All newly synthesized compounds were evaluated for their antimicrobial and antiproliferative activities. Our results showed that the benzimidazole-1,2,3-triazole-sulfonamide hybrids inhibited microbial and fungal strains within MIC values from 32 to 64 μg/mL. The antiproliferative evaluation of the synthesized compounds showed sufficient antiproliferative activities with IC

Indexed as

1,2,3-TriazolesADMETAntimicrobial activityAntiproliferative activityBenzimidazolesClick synthesisSulfonamides

Identifiers

PMID30387018
PMCPMC6768023

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.